This study develops a wavelet maxima-based methodology to extract anomalous signals from microwave brightness temperature (MBT) observations for seismic estimation. MBT, acquired via satellite microwave radiometry, enables subsurface characterization penetrating clouds. Five earthquake categories were defined contingent on locale (oceanic/terrestrial) and ambient traits (soil hydration, vegetal covering). Continuous wavelet transform was applied to preprocess annualized MBT readings preceding and succeeding prototypical events of each grouping, utilizing optimized wavelet functions and orders tailored to individualized contexts. Wavelet maxima graphs visually portraying signal intensity variations facilitated identification of aberrant phenomena, including pre-seismic accrual, co-seismic perturbation, and postsismic remission signatures. Casework found 10GHz horizontal-polarized MBT optimally detected signals for aquatic and predominantly humid/vegetative settings, whereas 36GHz horizontal-polarized performed best for arid, vegetated landmasses. This preliminary investigation establishes an analytical framework, albeit reliant on qualitative appraisals. Quantitative machine learning methods are warranted to statistically define selection standards and augment empirical forecasting leveraging lithospheric stress state inferences from sensitive MBT parametrization.

The Arbas cashmere goat is a unique biological resource that plays a vital role in livestock husbandry in China. LCDM is a medium with special small molecules (consisting of human LIF, CHIR99021, (S)-(+)-dimethindene maleate, and minocycline hydrochloride) for generation pluripotent stem cells (PSCs) with bidirectional developmental potential in mice, humans, pigs, and bovines. However, there is no report on whether LCDM can support for generation of PSCs with the same ability in Arbas cashmere goats. In this study, we applied LCDM to generation goat induced PSCs (giPSCs) from goat fetal fibroblasts (GFFs) by reprogramming. The derived giPSCs exhibited stem cell morphology, expressing pluripotent markers, and could differentiate into three germ layers. Moreover, the giPSCs differentiated into the trophectoderm lineage by spontaneous and directed differentiation in vitro. The giPSCs contributed to embryonic and extraembryonic tissue in preimplantation blastocysts and postimplantation chimeric embryos. RNA-sequencing analysis showed that the giPSCs were very close to goat embryos at the blastocyst stage and giPSCs have similar properties to typical extended PSCs (EPSCs). The establishment of giPSCs with LCDM provides a new way to generate high quality of PSCs from domestic animals and lays the foundation for basic and applied research in biology and agriculture.